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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 92953

1 recalled-product record grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
August 15, 2023
Product types
Food
Classifications
Class III
Statuses
Terminated
Recalling firm wording
Pharma-Natural Inc.

Dossier provenance

Source snapshots represented here

  • openFDA Food Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

1 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

food · product 1 of 1

Pharma Natural, Biotin 5000 mcg, Maximum Strength, Dietary Supplement, 30 Tablets

F-1615-2023
Recall number
F-1615-2023
Initiated
August 15, 2023
Classification
Class III
Status
Terminated
Recalling firm
Pharma-Natural Inc.
Quantity
204 bottles (102 twin packs)/30 tablets per bottle

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
FDA sample analysis of Pharma Natural Biotin 5000 mcg Maximum Strength (30 tablets, Lot: PN10686, Exp. Date 01/24), found the biotin content was below the detection limit.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

FDA sample analysis of Pharma Natural Biotin 5000 mcg Maximum Strength (30 tablets, Lot: PN10686, Exp. Date 01/24), found the biotin content was below the detection limit.

Code information

Lot: PN10686, Exp. Date 01/24

Distribution pattern

Puerto Rico

Field note

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